Protonated [4n]π and [4n+2]π Octaphyrins Choose Their Möbius/Hückel Aromatic Topology-Reference-Cited by-同舟云学术

Protonated [4n]π and [4n+2]π Octaphyrins Choose Their Möbius/Hückel Aromatic Topology

Published:2010-02-11 Issue:9 Volume:132 Page:3105-3114
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lim Jong Min¹,Shin Jae-Yoon¹,Tanaka Yasuo¹,Saito Shohei¹,Osuka Atsuhiro¹,Kim Dongho¹

Affiliation:

1. Spectroscopy Laboratory for Functional π-Electronic Systems and Department of Chemistry, Yonsei University, Seoul 120-749, Korea, and Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja909744z

Reference57 articles.

1. Topology in Chemistry: Designing Möbius Molecules

2. Aromatics with a twist

3. Möbius aromaticity and antiaromaticity in expanded porphyrins

4. Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch

5. Unambiguous Identification of Möbius Aromaticity for meso-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1)

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